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模拟微重力和超重对心肌细胞钙信号的影响。

Alteration of calcium signalling in cardiomyocyte induced by simulated microgravity and hypergravity.

机构信息

State Key Lab of Space Medicine Fundamentals and Application, China Astronaut Research and Training Center, Beijing, China.

Beijing National Day School, Beijing, China.

出版信息

Cell Prolif. 2020 Mar;53(3):e12783. doi: 10.1111/cpr.12783. Epub 2020 Feb 26.

Abstract

OBJECTIVES

Cardiac Ca signalling plays an essential role in regulating excitation-contraction coupling and cardiac remodelling. However, the response of cardiomyocytes to simulated microgravity and hypergravity and the effects on Ca signalling remain unknown. Here, we elucidate the mechanisms underlying the proliferation and remodelling of HL-1 cardiomyocytes subjected to rotation-simulated microgravity and 4G hypergravity.

MATERIALS AND METHODS

The cardiomyocyte cell line HL-1 was used in this study. A clinostat and centrifuge were used to study the effects of microgravity and hypergravity, respectively, on cells. Calcium signalling was detected with laser scanning confocal microscopy. Protein and mRNA levels were detected by Western blotting and real-time PCR, respectively. Wheat germ agglutinin (WGA) staining was used to analyse cell size.

RESULTS

Our data showed that spontaneous calcium oscillations and cytosolic calcium concentration are both increased in HL-1 cells after simulated microgravity and 4G hypergravity. Increased cytosolic calcium leads to activation of calmodulin-dependent protein kinase II/histone deacetylase 4 (CaMKII/HDAC4) signalling and upregulation of the foetal genes ANP and BNP, indicating cardiac remodelling. WGA staining indicated that cell size was decreased following rotation-simulated microgravity and increased following 4G hypergravity. Moreover, HL-1 cell proliferation was increased significantly under hypergravity but not rotation-simulated microgravity.

CONCLUSIONS

Our study demonstrates for the first time that Ca /CaMKII/HDAC4 signalling plays a pivotal role in myocardial remodelling under rotation-simulated microgravity and hypergravity.

摘要

目的

心脏 Ca 信号在调节兴奋-收缩偶联和心脏重构中起着至关重要的作用。然而,心肌细胞对模拟微重力和超重力的反应及其对 Ca 信号的影响尚不清楚。在这里,我们阐明了 HL-1 心肌细胞在旋转模拟微重力和 4G 超重力作用下增殖和重构的机制。

材料和方法

本研究使用心肌细胞系 HL-1。使用转椅和离心机分别研究微重力和超重力对细胞的影响。用激光扫描共聚焦显微镜检测 Ca 信号。通过 Western blot 和实时 PCR 分别检测蛋白质和 mRNA 水平。用小麦胚凝集素(WGA)染色分析细胞大小。

结果

我们的数据表明,在模拟微重力和 4G 超重力后,HL-1 细胞中的自发性钙振荡和胞质钙浓度均增加。胞质钙增加导致钙调蛋白依赖性蛋白激酶 II/组蛋白去乙酰化酶 4(CaMKII/HDAC4)信号的激活和胎儿基因 ANP 和 BNP 的上调,表明心脏重构。WGA 染色表明,旋转模拟微重力后细胞大小减小,4G 超重力后细胞大小增加。此外,HL-1 细胞增殖在超重力下显著增加,但在旋转模拟微重力下没有增加。

结论

本研究首次表明,Ca/CaMKII/HDAC4 信号在旋转模拟微重力和超重力下的心肌重构中起着关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3065/7106961/a80611485d7b/CPR-53-e12783-g001.jpg

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